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Mutations on the Protein: P05067 From Positions: 655 To 693

15
6
0
9


Swiss-Prot Disease: VAR_000016
p.ALA692GLY
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_044424
p.ASP678ASN
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Polymorphism: VAR_010107
p.GLU665ASP
N/A
N/A
N/A


Swiss-Prot Disease: VAR_000017
p.GLU693GLN
N/A
N/A
Cerebral amyloid angiopathy, APP-related (CAA-APP)


Swiss-Prot Disease: VAR_014215
p.GLU693GLY
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_014216
p.GLU693LYS
N/A
N/A
Cerebral amyloid angiopathy, APP-related (CAA-APP)


OMIM Disease: 104760.0005
p.ALA692GLY
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT||ALZHEIMER DISEASE, FAMILIAL, 1, INCLUDED


OMIM Disease: 104760.0023
p.ALA673THR
N/A
N/A
ALZHEIMER DISEASE, PROTECTION AGAINST


OMIM Disease: 104760.0022
p.ALA673VAL
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1, AUTOSOMAL RECESSIVE


OMIM Disease: 104760.0010
p.GLU665ASP
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0001
p.GLU693GLN
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT


OMIM Disease: 104760.0013
p.GLU693GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1||CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT, INCLUDED


OMIM Disease: 104760.0014
p.GLU693LYS
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT


OMIM Disease: 104760.0008
p.LYS670ASN
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0008
p.MET671LEU
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1






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